4.6 Article

Column coupling isotachophoresis-capillary electrophoresis with mass spectrometric detection: Characterization and optimization of microfluidic interfaces

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1297, Issue -, Pages 204-212

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2013.04.046

Keywords

Two-dimensional electrophoretic separations; ITP-CE; Microfluidic interfaces; Mass spectrometry; Contactless capacitively coupled conductivity detection; Numerical modeling

Funding

  1. Initiative and Networking Fund, Helmholtz Enterprise

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Two-dimensional electrophoretic separations are one of the most promising tools for the continuously growing needs of different bioanalytical fields such as proteomics and metabolomics. In this work we present the design and the implementation of a two-dimensional electrophoretic separation coupled to mass spectrometry. We started our work studying the sample transfer characteristics of different microfluidic interfaces compatible with capillary coupling for two-dimensional electrophoretic separations. These junctions are aimed at method decoupling and sample transfer in a modular two-dimensional electrophoretic separation system. In order to perform the characterization of the interfaces, we carried out capillary electrophoresis experiments and numerical simulations using three cationic compounds under different flow conditions. The comparison of the experimental and simulation results enables us to clearly define the desirable characteristics of interfaces in order to achieve method orthogonality with lossless sample transfer in a two-dimensional separation system. Finally, we present a glass microfluidic chip as interface for the implementation of a novel hybrid modular system for performing two-dimensional electrophoretic separations involving isotachophoresis and capillary electrophoresis. In this setup we include mass spectrometric and contactless capacitively coupled conductivity detection to monitor the separation process. We demonstrate the ability of the setup to be used as a flexible analysis tool by performing preconcentration, separation, detection and identification of four different human angiotensin peptides. (C) 2013 Elsevier B.V. All rights reserved.

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